A large number of industrially relevant enzymes depend upon nicotinamide cofactors, which are too expensive to be added in stoichiometric amounts. Existing NAD(P)H-recycling systems suffer from low activity, or the generation of side products. H₂-driven cofactor regeneration has the advantage of 100% atom efficiency and the use of H₂ as a cheap reducing agent, in a world where sustainable energy carriers are increasingly attractive. The state of development of H₂-driven cofactor-recycling systems and examples of their integration with enzyme reactions are summarized in this article. The O₂-tolerant NAD⁺-reducing hydrogenase from Ralstonia eutropha is a particularly attractive candidate for this approach, and we therefore discuss its catalytic properties that are relevant for technical applications.
Archaeal Proteins
,Bacterial Proteins
,Biocatalysis
,Bioreactors
,Cupriavidus necator
,Desulfovibrio
,Enzyme Stability
,Enzymes, Immobilized
,Hydrogen
,NAD
,NADP
,Oxidation-Reduction
,Oxidoreductases
,Reducing Agents